# Keller Laboratories - Inspection Records

Source: https://www.keypedia.com/companies/keller-laboratories/7cff8918-be58-467a-904d-3a4095742bc9

> Inspection records and compliance data for Keller Laboratories in Fenton, Missouri. Access full analysis and detailed observations.

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## Details

- Name: Keller Laboratories
- FEI Number: 3006650414
- City: Fenton
- State: Missouri
- Country Name: United States
- Address Line 1: 160 Larkin Williams Ind Ct
- Zip Code: 63026

## Related Documents

- [FDA Inspection 1311068 - Keller Laboratories - 2026-04-06](https://www.keypedia.com/records/fda_inspections/keller-laboratories/d2de8684-07df-47d4-839d-9cee33b48218) — source: FDA, date: April 6, 2026
- [FDA Inspection 1311068 - Keller Laboratories - 2026-04-06](https://www.keypedia.com/records/fda_inspections/keller-laboratories/e55ea529-969e-448e-9085-ad2379862424) — source: FDA, date: April 6, 2026
- [483 - Keller Laboratories - 2023-03-17](https://www.keypedia.com/records/483/keller-laboratories/d8ac52eb-74d2-467c-b61e-49e128d93e6b) — source: FDA, date: March 17, 2023
- [FDA Inspection 1200171 - Keller Laboratories - 2023-03-17](https://www.keypedia.com/records/fda_inspections/keller-laboratories/5352343e-26f5-4323-a2a4-c43d4d4bac3e) — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2023
- [FDA Inspection 1200171 - Keller Laboratories - 2023-03-17](https://www.keypedia.com/records/fda_inspections/keller-laboratories/412eee6f-cf87-4da3-8a7e-27a4605a7ac8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2023
- [FDA Inspection 1051759 - Keller Laboratories - 2018-05-10](https://www.keypedia.com/records/fda_inspections/keller-laboratories/5433423b-f6ec-4cd9-b659-81c600674989) — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2018
- [FDA Inspection 1051759 - Keller Laboratories - 2018-05-10](https://www.keypedia.com/records/fda_inspections/keller-laboratories/7917b00a-1542-441c-8c7a-52e2bfbe4616) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2018
- [FDA Inspection 882874 - Keller Laboratories - 2014-06-11](https://www.keypedia.com/records/fda_inspections/keller-laboratories/79223d74-ad6c-449b-8d5c-23fe034b5b81) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2014
- [FDA Inspection 882874 - Keller Laboratories - 2014-06-11](https://www.keypedia.com/records/fda_inspections/keller-laboratories/8531d71a-aac7-490f-8311-63264b421d82) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2014
- [FDA Inspection 787218 - Keller Laboratories - 2012-06-22](https://www.keypedia.com/records/fda_inspections/keller-laboratories/56ba50c2-c068-42ea-9cfd-b2398e6905fe) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 22, 2012
- [FDA Inspection 710510 - Keller Laboratories - 2011-02-11](https://www.keypedia.com/records/fda_inspections/keller-laboratories/8845274c-09c7-4270-9b32-f4dc7dc096ec) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 11, 2011

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## Related Officers

- [Edward E. Lockwood](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)